Identification of a novel frameshift mutation (383insT) in theRUNX2(PEBP2 α/CBFA1/AML3) gene in a Japanese patient with cleidocranial dysplasia
Masae Goseki-Sone, Hideo Orimo, Atsushi Watanabe, Ryoko Hamatani, Masahiko Yokozeki, Kimie Ohyama, Takayuki Kuroda, Hisashi Watanabe, Hidetaka Miyazaki, Takashi Shimada, Shinichiro OidaVolume:
19
Langue:
english
Pages:
4
DOI:
10.1007/s007740170030
Date:
July, 2001
Fichier:
PDF, 370 KB
english, 2001
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